홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Azide → 3-(4-Chlorobenzoyl)-benzyl azide

HRID 280637
노트
인쇄 미리보기

반응식

HRID 280637 반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH2:11]Br)=[O:7])=[CH:4][CH:3]=1.[N-:18]=[N+:19]=[N-:20].[Na+]>C(O)C>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[CH2:11][N:18]=[N+:19]=[N-:20])=[O:7])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 136496533-(4-Chlorobenzoyl)benzyl bromide

생성물 1

HCID 136496603-(4-Chlorobenzoyl)-benzyl azide수율 100.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 3-(4-chlorobenzoyl)benzyl bromide (4.2 g, 13.6 mmol) and sodium azide (1.32 g, 20.3 mmol) in ethanol (40 ml) was refluxed for 5 hours, cooled to ambient temperature, and kept 16 hours. The mixture was filtered and the solids were washed twice with ethanol. The combined filtrate and washes were evaporated to dryness under vacuum and the residue was treated with diethyl ether and filtered. The filtrate was evaporated to dryness under vacuum and dried to provide 3.7 g (100%) of 3-(4-chlorobenzoyl)-benzyl azide, m.p. 43°-45° C.

후처리

  1. temperaturewas refluxed for 5 hours
  2. filtrationThe mixture was filtered
  3. washthe solids were washed twice with ethanol
  4. customThe combined filtrate and washes were evaporated to dryness under vacuum
  5. additionthe residue was treated with diethyl ether
  6. filtrationfiltered
  7. customThe filtrate was evaporated to dryness under vacuum
  8. customdried

출처 및 근거

ORD 기록
ord-797ab928d8754b319797ffa3ce390464
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04590201

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트